Background and aim: Systemic inflammation is related to the progression of complications associated with diabetes. This study aimed to investigate the association between general and abdominal obesity and inflammation in patients with type-2 diabetes with or without glycemic control. Methods: A total of 198 men (n=73) and women (n=125) diagnosed with type 2 diabetes participated in this study. General obesity markers, body mass index (BMI), and abdominal fat were assessed. Circulating concentrations of glycated hemoglobin (HbA1C), C-reactive protein (CRP), and serum interleukin-6 (IL-6) were determined. Poor glycemic control and good glycemic control were defined as having fasting HbA1C concentrations >= 7% and <7%, respectively. Multivariate adjusted analysis of covariance was used to determine the relation between BMI and abdominal fat and markers of inflammation in patients with good and poor glycemic control. Results: Patients in <7% HbA1C category, those with high abdominal fat had approximate to 262% higher CRP and approximate to 30.6% higher IL-6 compared to those with low abdominal fat (p<0.05). Patients in >= 7% HbA1C category, those with high abdominal fat had approximate to 41.4% higher CRP and approximate to 33.9% higher IL-6 compared to those with low abdominal fat (p<0.05). Abdominal fat was directly related to CRP (p<0.023) and IL-6 (p<0.002) concentrations in both groups of type-2 diabetic patients with <7% and >= 7% HbA1C. In patients with >= 7% HbA1C, BMI was directly related to CRP (p<0.02) and IL-6 (p<0.047). Whereas in patients with <7% HbA1C, BMI was not associated with CRP or IL-6 concentrations. Conclusion: High level of abdominal fat is associated with systemic inflammation in type-2 diabetes regardless of glycemic control. Abdominal fat is a better predictor (determinant) of inflammation than BMI in patients with type-2 diabetes with or without glycemic control.
机构:
Univ Virginia, Dept Biomed Engn, Charlottesville, VA 22904 USA
Univ Virginia, Ctr Publ Hlth Genom, Charlottesville, VA 22904 USAUniv Virginia, Dept Biomed Engn, Charlottesville, VA 22904 USA
Aberra, Yonathan Tamrat
Ma, Lijiang
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Icahn Sch Med Mt Sinai, Dept Genet & Genom Sci, New York, NY 10029 USAUniv Virginia, Dept Biomed Engn, Charlottesville, VA 22904 USA
Ma, Lijiang
Bjorkegren, Johan L. M.
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Icahn Sch Med Mt Sinai, Dept Genet & Genom Sci, New York, NY 10029 USA
Karolinska Inst, Dept Med, Huddinge, SwedenUniv Virginia, Dept Biomed Engn, Charlottesville, VA 22904 USA
Bjorkegren, Johan L. M.
Civelek, Mete
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Univ Virginia, Dept Biomed Engn, Charlottesville, VA 22904 USA
Univ Virginia, Ctr Publ Hlth Genom, Charlottesville, VA 22904 USAUniv Virginia, Dept Biomed Engn, Charlottesville, VA 22904 USA